scholarly journals Metastasizing Malignant Granular Cell Tumor (Abrikossoff Tumor) of the Anterior Abdominal Wall, with Prolonged Survival

2019 ◽  
Vol 2019 ◽  
pp. 1-8
Author(s):  
Yara A. Alnashwan ◽  
Khaled A. H. Ali ◽  
Samir S. Amr

Malignant granular cell tumor (MGCT) is a rare high-grade mesenchymal tumor of Schwann cell origin. MGCTs commonly affect thigh, extremity, and trunk; however, involvement of the abdominal wall is quite rare. It has poor prognosis with 39% mortality rate in 3-year interval. We report a 50-year-old female who had MGCT arising in the anterior abdominal wall and developed massive metastatic deposits in both lungs and in the right inguinal lymph nodes, with prolonged survival for 11 years. A brief review of the literature is presented.

2012 ◽  
Vol 7 (3) ◽  
pp. 716 ◽  
Author(s):  
Lee J. McGhan ◽  
Nabil Wasif ◽  
Scott W. Young ◽  
Joseph M. Collins ◽  
Ann E. McCullough

2015 ◽  
Vol 10 (2) ◽  
pp. 972-974 ◽  
Author(s):  
SACHI MORITA ◽  
MARIKO HIRAMATSU ◽  
MIHOKO SUGISHITA ◽  
BISHAL GYAWALI ◽  
TAKASHI SHIBATA ◽  
...  

1998 ◽  
Vol 194 (7) ◽  
pp. 507-513 ◽  
Author(s):  
Hiroshi Sonobe ◽  
Jun Iwata ◽  
Mutsuo Furihata ◽  
Toshiaki Moriki ◽  
Yuji Ohtsuki

2021 ◽  
Vol 8 (1) ◽  
pp. 27
Author(s):  
Sei Morinaga ◽  
Norio Yamamoto ◽  
Katsuhiro Hayashi ◽  
Akihiko Takeuchi ◽  
Shinji Miwa ◽  
...  

Background: The incidence of malignant granular cell tumor, an extremely rare Schwann cell-derived tumor with a poor prognosis, is reported to be approximately 0.2% of malignant soft tissue tumors. We report a case of a malignant granular cell tumor originating from the ulnar nerve.Case presentation: A 71-year-old woman presented with a mass in her right forearm. Magnetic resonance imaging showed a tumor with homogenous intensity of T1 and heterogeneous hyperintensity of T2, continuous with the ulnar nerve. Incisional biopsy revealed a malignant granular cell tumor, and marginal excision of the tumor was performed. Histologically, the tumor size was 9.2 cm and consisted of eosinophilic, granular polygonal to round and spindle-shaped cells, with vesicular and prominent nucleoli, and increased mitosis. Immunohistochemically, the tumor cells were positive for S-100 protein, CD68, H3K27me3, TFE3, and SOX10 and negative for smooth muscle alpha-actin, desmin, cytokeratin AE1/3, epithelial membrane antigen, and synaptophysin. The Ki-67 positivity rate was 12%. These findings were consistent with those of malignant granular cell tumors. In addition, no metastasis or recurrence was observed 15 years after the excision.Conclusion: Surgical resection is the standard treatment option. In our case, the diagnostic criteria for malignant granular cell tumors were histologically met. Patients with malignant granular cell tumors have a poor prognosis. However, no metastasis or recurrence was observed in this case 15 years after the surgery.


2012 ◽  
Vol 4 (1) ◽  
pp. 63-66 ◽  
Author(s):  
JIDA CHEN ◽  
LINBO WANG ◽  
JING XU ◽  
TAO PAN ◽  
JIANGUO SHEN ◽  
...  

1988 ◽  
Vol 49 (5) ◽  
pp. 825-832
Author(s):  
Akiteru HAYASHI ◽  
Shigehiko KABURAGI ◽  
Kyoei NONAKA ◽  
Tadaaki SHIBA ◽  
Setsuo TAKEUCHI ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document